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      Mechanisms for estrogen receptor expression in human cancer

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          Abstract

          Estrogen is a steroid hormone that has critical roles in reproductive development, bone homeostasis, cardiovascular remodeling and brain functions. However, estrogen also promotes mammary, ovarian and endometrial tumorigenesis. Estrogen antagonists and drugs that reduce estrogen biosynthesis have become highly successful therapeutic agents for breast cancer patients. The effects of estrogen are largely mediated by estrogen receptor (ER) α and ERβ, which are members of the nuclear receptor superfamily of transcription factors. The mechanisms underlying the aberrant expression of ER in breast cancer and other types of human tumors are complex, involving considerable alternative splicing of ERα and ERβ, transcription factors, epigenetic and post-transcriptional regulation of ER expression. Elucidation of mechanisms for ER expression may not only help understand cancer progression and evolution, but also shed light on overcoming endocrine therapy resistance. Herein, we review the complex mechanisms for regulating ER expression in human cancer.

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            Cloning of a novel receptor expressed in rat prostate and ovary.

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              Gata-3 is an essential regulator of mammary-gland morphogenesis and luminal-cell differentiation.

              The transcription factor Gata-3 is a defining marker of the 'luminal' subtypes of breast cancer. To gain insight into the role of Gata-3 in breast epithelial development and oncogenesis, we have explored its normal function within the mammary gland by conditionally deleting Gata-3 at different stages of development. We report that Gata-3 has essential roles in the morphogenesis of the mammary gland in both the embryo and adult. Through the discovery of a novel marker (beta3-integrin) of luminal progenitor cells and their purification, we demonstrate that Gata-3 deficiency leads to an expansion of luminal progenitors and a concomitant block in differentiation. Remarkably, introduction of Gata-3 into a stem cell-enriched population induced maturation along the alveolar luminal lineage. These studies provide evidence for the existence of an epithelial hierarchy within the mammary gland and establish Gata-3 as a critical regulator of luminal differentiation.
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                Author and article information

                Contributors
                huahuihuaxi@163.com
                695828920@qq.com
                kongqingbincdut@163.com
                jyangfu@scu.edu.cn
                Journal
                Exp Hematol Oncol
                Exp Hematol Oncol
                Experimental Hematology & Oncology
                BioMed Central (London )
                2162-3619
                19 September 2018
                19 September 2018
                2018
                : 7
                : 24
                Affiliations
                [1 ]ISNI 0000 0004 1770 1022, GRID grid.412901.f, Laboratory of Stem Cell Biology, , West China Hospital, Sichuan University, ; Chengdu, China
                [2 ]ISNI 0000 0004 1770 1022, GRID grid.412901.f, Laboratory of Oncogene, , West China Hospital, Sichuan University, ; Chengdu, China
                Article
                116
                10.1186/s40164-018-0116-7
                6148803
                30250760
                f8c83da0-214b-4639-9ce7-25e7514b0e16
                © The Author(s) 2018

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

                History
                : 19 July 2018
                : 12 September 2018
                Categories
                Review
                Custom metadata
                © The Author(s) 2018

                Oncology & Radiotherapy
                cancer,estrogen receptor,transcription,epigenetic modification
                Oncology & Radiotherapy
                cancer, estrogen receptor, transcription, epigenetic modification

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